借鉴历史研究的贝叶斯混合设计。

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pharmaceutical Statistics Pub Date : 2024-12-27 DOI:10.1002/pst.2466
Zhaohua Lu, John Toso, Girma Ayele, Philip He
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引用次数: 0

摘要

在联合治疗的早期药物开发中,主要目的是初步评估当一种新药物与一种既定的单一疗法联合使用时,是否有添加性活性。由于进行大型随机研究的潜在可行性问题,非对照单臂试验一直是癌症临床试验的主流方法。然而,由于传统的双臂试验缺乏随机化,这类试验在决定是否进行下一阶段的开发时往往面临重大挑战。混合设计,利用来自单一疗法的完整历史临床研究的数据,为提高研究效率和改善知情决策提供了有价值的选择。与传统的单臂设计相比,混合设计可以通过借鉴外部信息显着提高功率,从而实现更可靠的活动评估。混合设计的主要挑战在于如何处理信息借用。我们引入了一个贝叶斯动态功率先验框架,该框架包含三个控制动态借贷量的组件。该框架提供了灵活的学习设计选项,明确解释了借用,允许根据特定需求进行定制。此外,该框架中的后验分布具有封闭形式,在计算效率方面具有显著优势。通过仿真和案例研究证明了该框架的实用性。
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A Bayesian Hybrid Design With Borrowing From Historical Study.

In early phase drug development of combination therapy, the primary objective is to preliminarily assess whether there is additive activity from a novel agent when combined with an established monotherapy. Due to potential feasibility issues for conducting a large randomized study, uncontrolled single-arm trials have been the mainstream approach in cancer clinical trials. However, such trials often present significant challenges in deciding whether to proceed to the next phase of development due to the lack of randomization in traditional two-arm trials. A hybrid design, leveraging data from a completed historical clinical study of the monotherapy, offers a valuable option to enhance study efficiency and improve informed decision-making. Compared to traditional single-arm designs, the hybrid design may significantly enhance power by borrowing external information, enabling a more robust assessment of activity. The primary challenge of hybrid design lies in handling information borrowing. We introduce a Bayesian dynamic power prior (DPP) framework with three components of controlling amount of dynamic borrowing. The framework offers flexible study design options with explicit interpretation of borrowing, allowing customization according to specific needs. Furthermore, the posterior distribution in the proposed framework has a closed form, offering significant advantages in computational efficiency. The proposed framework's utility is demonstrated through simulations and a case study.

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来源期刊
Pharmaceutical Statistics
Pharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.70
自引率
6.70%
发文量
90
审稿时长
6-12 weeks
期刊介绍: Pharmaceutical Statistics is an industry-led initiative, tackling real problems in statistical applications. The Journal publishes papers that share experiences in the practical application of statistics within the pharmaceutical industry. It covers all aspects of pharmaceutical statistical applications from discovery, through pre-clinical development, clinical development, post-marketing surveillance, consumer health, production, epidemiology, and health economics. The Journal is both international and multidisciplinary. It includes high quality practical papers, case studies and review papers.
期刊最新文献
A Commensurate Prior Model With Random Effects for Survival and Competing Risk Outcomes to Accommodate Historical Controls. Bayesian Sample Size Calculation in Small n, Sequential Multiple Assignment Randomized Trials (snSMART). Taylor Series Approximation for Accurate Generalized Confidence Intervals of Ratios of Log-Normal Standard Deviations for Meta-Analysis Using Means and Standard Deviations in Time Scale. A Bayesian Hybrid Design With Borrowing From Historical Study. WATCH: A Workflow to Assess Treatment Effect Heterogeneity in Drug Development for Clinical Trial Sponsors.
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